A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603434



Internal ID16390843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65329708..65373887hg38UCSC Ensembl
Innerchr6:66039601..66083780hg19UCSC Ensembl
Innerchr6:66096322..66140501hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3844180
hg1944180
hg1844180
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10725n54
Supporting Variantsnssv1153707
Samples1787431198_A
Known GenesEYS
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603434
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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